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SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K052810
510(k) Type
Traditional
Applicant
SCANDIUS BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2005
Days to Decision
77 days
Submission Type
Summary

SCANDIUS TRITIS TIBIAL ACL RECONSTRUCTION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K052810
510(k) Type
Traditional
Applicant
SCANDIUS BIOMEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2005
Days to Decision
77 days
Submission Type
Summary